VivaDiag™ Methamphetamine Test Kit (FIA) - Indonesia BPOM Medical Device Registration
VivaDiag™ Methamphetamine Test Kit (FIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320617. The device is manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CAKRA MEDIKA UTAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
VIVACHEK BIOTECH (HANGZHOU) CO., LTDCountry of Origin
China
Authorized Representative
CAKRA MEDIKA UTAMAAR Address
FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon
Registration Date
Nov 21, 2023
Expiry Date
Sep 10, 2025
Product Type
Clinical Toxicology Test System
Methamphetamine test system(card)
Invitro Diagnostics
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VivaDiag ™ Plus Hemoglobin Testing System
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